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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 2
1979 1
1983 3
1984 1
1985 2
1990 1
1991 2
1992 3
1993 6
1994 3
1995 5
1996 5
1997 3
1998 19
1999 5
2000 6
2001 8
2002 8
2003 3
2004 8
2005 8
2006 3
2007 11
2008 9
2009 9
2010 15
2011 13
2012 6
2013 5
2014 12
2015 9
2016 20
2017 10
2018 8
2019 13
2020 18
2021 24
2022 15
2023 11
2024 0

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PubMed for id: 419152

294 results

Results by year

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Page 1
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI).
Serrano-Lorenzo P, Rabasa M, Esteban J, Hidalgo Mayoral I, Domínguez-González C, Blanco-Echevarría A, Garrido-Moraga R, Lucia A, Blázquez A, Rubio JC, Palma-Milla C, Arenas J, Martín MA. Serrano-Lorenzo P, et al. Genes (Basel). 2022 Oct 11;13(10):1835. doi: 10.3390/genes13101835. Genes (Basel). 2022. PMID: 36292720 Free PMC article.
The SGLT2 inhibitor dapagliflozin improves kidney function in glycogen storage disease XI.
Trepiccione F, Iervolino A, D'Acierno M, Siccardi S, Costanzo V, Sardella D, De La Motte LR, D'Apolito L, Miele A, Perna AF, Capolongo G, Zacchia M, Frische S, Nielsen R, Staiano L, Sambri I, De Cegli R, Unwin R, Eladari D, Capasso G. Trepiccione F, et al. Sci Transl Med. 2023 Nov;15(720):eabn4214. doi: 10.1126/scitranslmed.abn4214. Epub 2023 Nov 1. Sci Transl Med. 2023. PMID: 37910600
Assessment of the diagnosis, treatment, and follow-up of a group of Turkish pediatric glycogen storage disease type 1b patients with varying clinical presentations and a novel mutation.
Küçükçongar Yavaş A, Engin Erdal A, Bilginer Gürbüz B, Ünlüsoy Aksu A, Kasapkara ÇS. Küçükçongar Yavaş A, et al. J Pediatr Endocrinol Metab. 2023 Oct 5;36(11):1092-1099. doi: 10.1515/jpem-2023-0336. Print 2023 Nov 27. J Pediatr Endocrinol Metab. 2023. PMID: 37791580
Clinical and genetic spectrum of GSD type 6 in Korea.
Hahn JW, Lee H, Seong MW, Kang GH, Moon JS, Ko JS. Hahn JW, et al. Orphanet J Rare Dis. 2023 Jun 1;18(1):132. doi: 10.1186/s13023-023-02750-1. Orphanet J Rare Dis. 2023. PMID: 37264426 Free PMC article.
294 results